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13006-59-2

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13006-59-2 Usage

General Description

1H-Indole-2-carbonitrile, 3-methyl- is a chemical compound with the molecular formula C10H8N2. It is a derivative of indole and is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. 1H-Indole-2-carbonitrile,3-methyl- is found in a wide variety of applications, including as a precursor for the production of dyes and pigments, as well as in the development of new materials. Additionally, 1H-Indole-2-carbonitrile, 3-methyl- has been studied for its potential biological activities, including its anticancer and anti-inflammatory properties. Overall, this chemical compound plays a significant role in various industrial and research applications due to its versatile properties and potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 13006-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13006-59:
(7*1)+(6*3)+(5*0)+(4*0)+(3*6)+(2*5)+(1*9)=62
62 % 10 = 2
So 13006-59-2 is a valid CAS Registry Number.

13006-59-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1H-indole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Cyano-3-methylindol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13006-59-2 SDS

13006-59-2Relevant articles and documents

An unusual reaction of skatole with tetranitromethane.

Spande,Fontana,Witkop

, p. 6199 - 6200 (1969)

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Yoshida

, p. 6111,6112 (1977)

-

Intermolecular reactions of indol-2-yl radicals: A new route to 2-substituted indoles

Fiumana, Andrea,Jones, Keith

, p. 1761 - 1762 (2007/10/03)

The generation of indol-2yl radicals and their addition to a variety of radical accepters to prepare 2-substituted indoles is presented.

Thermochemical Behavior of o-Azidocinnamonitriles

Garanti, Luisa,Zecchi, Gaetano

, p. 4767 - 4769 (2007/10/02)

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